Cxcl9 Variant Search Result - Rat Genome Database

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15 records found for search term Cxcl9

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329387918	CV2468482	single nucleotide variant	NM_002416.3(CXCL9):c.74T>C (p.Val25Ala)	not specified [RCV004278065]	uncertain significance	4	76006265	76006265	Human		name
405665624	CV3243230	single nucleotide variant	NM_002416.3(CXCL9):c.32G>A (p.Gly11Asp)	not specified [RCV004367583]	uncertain significance	4	76007418	76007418	Human		name
598236667	CV3956183	single nucleotide variant	NM_002416.3(CXCL9):c.89G>A (p.Arg30His)	not specified [RCV005320482]	uncertain significance	4	76006250	76006250	Human		name
15185772	CV721068	single nucleotide variant	NM_002416.3(CXCL9):c.375A>G (p.Thr125=)	not provided [RCV000886789]	benign	4	76003601	76003601	Human		name
155919688	CV2202715	single nucleotide variant	NM_002416.3(CXCL9):c.175G>A (p.Glu59Lys)	not specified [RCV004082960]	uncertain significance	4	76006164	76006164	Human		name
156068080	CV2317965	single nucleotide variant	NM_002416.3(CXCL9):c.154T>G (p.Phe52Val)	not specified [RCV004177085]	uncertain significance	4	76006185	76006185	Human		name
401736579	CV2703186	single nucleotide variant	NM_002416.3(CXCL9):c.236C>T (p.Ser79Leu)	not specified [RCV004315251]	uncertain significance	4	76004849	76004849	Human		name
401890778	CV2772160	single nucleotide variant	NM_002416.3(CXCL9):c.290A>C (p.Lys97Thr)	not specified [RCV004344809]	uncertain significance	4	76003686	76003686	Human		name
401862438	CV2775301	single nucleotide variant	NM_002416.3(CXCL9):c.209G>C (p.Gly70Ala)	not specified [RCV004348418]	uncertain significance	4	76004876	76004876	Human		name
405665614	CV3243228	single nucleotide variant	NM_002416.3(CXCL9):c.103A>G (p.Ser35Gly)	not specified [RCV004367581]	uncertain significance	4	76006236	76006236	Human		name
597655328	CV3657910	single nucleotide variant	NM_002416.3(CXCL9):c.134C>T (p.Ser45Phe)	not specified [RCV004911038]	uncertain significance	4	76006205	76006205	Human		name
15202129	CV749061	single nucleotide variant	NM_002416.3(CXCL9):c.119C>G (p.Thr40Ser)	not provided [RCV000913344]	likely benign	4	76006220	76006220	Human		name
405665620	CV3243229	single nucleotide variant	NM_002416.3(CXCL9):c.311A>C (p.Lys104Thr)	not specified [RCV004367582]	uncertain significance	4	76003665	76003665	Human		name
405665629	CV3243231	single nucleotide variant	NM_002416.3(CXCL9):c.341G>A (p.Arg114Gln)	not specified [RCV004367584]	uncertain significance	4	76003635	76003635	Human		name
597655320	CV3657909	single nucleotide variant	NM_002416.3(CXCL9):c.353G>A (p.Arg118His)	not specified [RCV004911037]	uncertain significance	4	76003623	76003623	Human		name